Associative processes in adaptation to repeated cold exposure in rats.

Learning processes have been implicated in drug tolerance, but the role of associative mechanisms in adaptation to stressors has not previously been determined. Rats that received daily brief cold exposures demonstrated adaptation to the cold as measured by an attenuation of hypothermia. Tolerance to the cold was disrupted by changing the context in which the subject experienced the cold. These findings provide evidence of associative processes in adaptation to cold exposure and illustrate that these processes are not limited to drug tolerance.

State-dependent retention produced with estrus in rats.

State-dependent retention (SDR) has frequently been demonstrated with drug-induced physiological changes which apparently serve as contextual cues for memory. These support the assumption that commonly occurring endogenous dispositions play a role in memory, yet there are few reports showing SDR with states that are likely to be part of an organism's natural experiences. To determine if behavioral estrus could produce SDR, ovariectomized female rats were rendered estrus via hormone injections or remained anestrus via placebo injections, trained with quinine-laced apple juice, and later tested while in the same or different state for reactions towards pure juice. SDR was not evident in the amount of juice consumed; however, those tested in the same state as the initial experience were slower to initiate drinking than those tested in a different state revealing a state-dependent influence on memory related to phases of the ovarian cycle.

Inaccuracies associated with the automated measurement of mean cell hemoglobin concentration in dehydrated cells.

Because of discrepancies between electronically and manually measured values of mean cell hemoglobin concentration (MCHC) encountered in studies of pathologic red cells, we studied the effect of cell water content on MCHC measurements by both methods. A series of red cell samples with varying water contents (54%-164% normal) were prepared from normal cells using the antibiotic nystatin. MCHC was then measured, using the microhematocrit centrifuge and three different electronic cell counters in common laboratory use. For MCHC values above 36 g/dl as measured by the spun hematocrit method, all three electronic counters under estimmated the MCHC, with increasing error as the true MCHC increased. For MCHC values below 30 g/dl, the values from two conductivity based instruments agreed with those from the spun hematocrit method, whereas one instrument based on light scattering overestimated the MCHC. These results indicate that inaccuracies in the measured mean cell volume (MCV) of dehydrated or otherwise undeformable cells may lead to spurious values for MCHC when electronic cell counters are used.